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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358396Generated: October 29, 2026

Ethanol → 5-benzyl-6-methyl-2-methylsulfanyl-1H-pyrimidin-4-one

https://huagongshe.com/reaction/358396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
Reactant5-Benzyl-6-methylthiouracilHCID 697326—
SolventWaterHCID 962—
Product5-benzyl-6-methyl-2-methylsulfanyl-1H-pyrimidin-4-oneHCID 135422583—

Reaction Conditions

Temperature60 °C

Reaction Steps

5-Benzyl-6-methylthiouracil (6.0 gms) and sodium hydroxide (1.06 gms) were dissolved in water (30 mls). The solution was cooled and ethanol (60 mls) and methyl iodide (3.67 gms) added with stirring. The mixture was heated at 60° C. for 1/2 hour, cooled and the resulting solid collected and water-washed. A second crop of solid was obtained by acidification of the filtrate to pH=4 with acetic acid. Recrystallisation from ethanol produced 5-benzyl-6-methyl-2-methylthio-4-pyrimidone (5.53 gms) m.p.=220°-221.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04467087
Source datasetuspto-grants-1984_08
ORD IDord-ca3e2220b240409c9da9435e3a639bb9
Source noteuspto-grants-1984_08